Elsevier

Human Pathology

Volume 13, Issue 10, October 1982, Pages 911-915
Human Pathology

Pulmonary veno-occlusive disease in siblings: Case reports and morphometric study

https://doi.org/10.1016/S0046-8177(82)80051-8Get rights and content

Two cases of fatal veno-occlusive disease are described: the first in a boy 14 years old and the second in his sister, who died, at age 13, only a few months later. In both, the first symptom was effort-induced dyspnea and the course of the disease was rapid. The chest radiograph of the boy showed diffuse opacities, whereas that of the girl showed Kerley lines bilaterally. In both, at autopsy, a diagnosis of severe veno-occlusive disease was confirmed, with partial or complete occlusion of much of the pulmonary venous bed by organized thrombi. The pulmonary vascular system of the girl was processed for light microscopic morphometry by injection of radiopaque medium into the veins of one lung and the arteries of the other. Although there was little filling of the venous system, much of the arterial system filled down to the capillary level. Pre-acinar and intra-acinar arteries showed medial hypertrophy and extension of smooth muscle into precapillary arteries. The concentration of patent intra-acinar arteries relative to alveoli was not significantly less than normal, whereas the concentration of veins was strikingly reduced. Possible pathogenetic mechanisms are discussed.

References (25)

  • WagenvoortCA

    Pulmonary veno-occlusive disease: entity or syndrome?

    Chest

    (1976)
  • CarringtonCB et al.

    Pulmonary veno-occlusive disease

    Hum Pathol

    (1970)
  • RosenthalA et al.

    Intra-pulmonary veno-occlusive disease

    Am J Cardiol

    (1973)
  • CraneJT et al.

    Isolated pulmonary venous sclerosis: a cause of cor pulmonale

    J Thorac Cardiovasc Surg

    (1960)
  • DailDH et al.

    A study of 43 cases of pulmonary veno-occlusive disease

    Lab Inest

    (1978)
  • LiebowAA et al.

    Rapidly progressive dyspnea in a teenage boy

    JAMA

    (1973)
  • CorrinB et al.

    Pulmonary veno-occlusion: an immune complex disease?

    Virchows Arch [Pathol Anat]

    (1974)
  • WagenvoortCA

    Wagenvoort N: The pathology of pulmonary veno-occlusive disease

    Virchows Arch [Pathol Anat]

    (1974)
  • HislopA et al.

    Pulmonary arterial development during childhood: branching pattern and structure

    Thorax

    (1973)
  • HislopA

    The fetal and childhood development of the pulmonary circulation and its disturbance in certain types of congenital heart disease

  • HislopA et al.

    Quantitative structural analysis of pulmonary vessels in isolated ventricular septal defect in infancy

    Br Heart J

    (1975)
  • DarocaPJ et al.

    Pulmonary venoocclusive disease: reports of a case with pseudoangiomatous features

    Am J Surg Pathol

    (1977)
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    Received from the Department of Pathology, Children's Hospital Medical Center and Harvard Medical School, Boston, Massachusetts.

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